Adsorptive-dissolution of O2 into the potential nanospace of a densely fluorinated metal-organic framework

Nanoporous solids, including metal-organic frameworks (MOFs), have long been known to capture small molecules by adsorption on their pore surfaces. Liquids are also known to accommodate small molecules by dissolution. These two processes have been recognized as fundamentally distinct phenomena because of the different nature of the medium-solids and liquids. Here, we report a dissolution-like gas accommodation so-called "adsorptive-dissolution" behavior in a MOF (PFAC-2) with pores densely filled with perfluoroalkyl chains. PFAC-2 does not have solvent-accessible voids; nevertheless, it captures oxygen molecules without changing the framework structure, analogous to molecular dissolution into liquids. Moreover, we demonstrate the selective capture of O<sub>2</sub> by PFAC-2 in a mixture of O<sub>2</sub> and Ar, which are difficult to separate due to their similarities such as boiling point and molecular size. Our results show the integration of molecular adsorption into nanospaces and dissolution into fluorous solvents, which can guide the design of crystalline adsorbents for selective molecular trapping and gas separation.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2024-11-22
DOI
https://doi.org/10.1038/s41467-024-54391-y
Citations
11
Primary Topic
Metal-Organic Frameworks: Synthesis and Applications
Type
article
Field-Weighted Citation Impact
1.74

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Adsorptive-dissolution of O2 into the potential nanospace of a densely fluorinated metal-organic framework

Jenny Pirillo, Junichi Usuba, Yuh Hijikata, Ryotaro Matsuda et al.
11 citations
Nature Communications
Metal-Organic Frameworks: Synthesis and Applications
1.74
article

Adsorptive-dissolution of O2 into the potential nanospace of a densely fluorinated metal-organic framework

Jenny Pirillo, Junichi Usuba, Yuh Hijikata, Ryotaro Matsuda, Yoshiteru Itoh, Yun‐Sheng Ma, Akihiro Hori, Shinpei Kusaka
article en
11 citations

Abstract

Nanoporous solids, including metal-organic frameworks (MOFs), have long been known to capture small molecules by adsorption on their pore surfaces. Liquids are also known to accommodate small molecules by dissolution. These two processes have been recognized as fundamentally distinct phenomena because of the different nature of the medium-solids and liquids. Here, we report a dissolution-like gas accommodation so-called "adsorptive-dissolution" behavior in a MOF (PFAC-2) with pores densely filled with perfluoroalkyl chains. PFAC-2 does not have solvent-accessible voids; nevertheless, it captures oxygen molecules without changing the framework structure, analogous to molecular dissolution into liquids. Moreover, we demonstrate the selective capture of O<sub>2</sub> by PFAC-2 in a mixture of O<sub>2</sub> and Ar, which are difficult to separate due to their similarities such as boiling point and molecular size. Our results show the integration of molecular adsorption into nanospaces and dissolution into fluorous solvents, which can guide the design of crystalline adsorbents for selective molecular trapping and gas separation.

Nature CommunicationsVol. 15(1)
Suzhou University of Technology (CN), Nagoya University (JP)
Japan Society for the Promotion of Science, Japan Science and Technology Agency, Core Research for Evolutional Science and Technology, Precursory Research for Embryonic Science and Technology, Co-creation place formation support program
Openalex Percentile: Top 16%
Metal-Organic Frameworks: Synthesis and Applications
1.74
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.